You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations
Job Summary
You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations.
ICON plc is a world-leading healthcare intelligence and clinical research organization.
Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Matching Summary
You will oversee site start-up and activation workstreams, ensuring deliverables meet quality and timeline expectations.
Skills & Requirements
Must-have
Feasibility and Site Activation (FSA)
clinical study start-up
manage project plans and timelines
essential document collection
ethics and regulatory submissions
site activation milestones
Nice-to-have
foster an inclusive environment
process improvement and best practice sharing
develop your team
customer satisfaction
Key Requirements
Bachelor's degree or equivalent experience
Strong experience in clinical research
Proven ability to manage project plans
Good understanding of regulatory requirements
Excellent communication and stakeholder management skills